A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6328033



Internal ID20861177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:11854955..11859433hg38UCSC Ensembl
chr1:11915012..11919490hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg384479
hg194479
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18051178
Samples
Known GenesNPPB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6328033
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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